Skip to main navigation Skip to search Skip to main content

Cerebral perfusion differences in the visual cortex and fusiform subregions across the psychosis spectrum

  • Jothini Sritharan
  • , Victor Zeng
  • , Jan Petr
  • , Henk-Jan Mutsaerts
  • , Dung Hoang
  • , Nicolas R. Bolo
  • , Elena I. Ivleva
  • , Weiying Dai
  • , Elliot S. Gershon
  • , Sarah K. Keedy
  • , David A. Parker
  • , Rebekah L. Trotti
  • , Jennifer E. McDowell
  • , Brett A. Clementz
  • , Carol A. Tamminga
  • , Godfrey D. Pearlson
  • , Matcheri S. Keshavan
  • , Paulo Lizano*
  • *Corresponding author for this work
  • Swiss Paraplegic Centre
  • Swiss Federal Institute of Technology Zurich
  • Beth Israel Deaconess Medical Center
  • Helmholtz-Zentrum Dresden-Rossendorf
  • Amsterdam UMC - Vrije Universiteit Amsterdam
  • Amsterdam UMC
  • Harvard University
  • University of Texas Southwestern Medical Center
  • State University of New York Binghamton University
  • The University of Chicago
  • University of Georgia
  • Institute of Living
  • Yale University

Research output: Contribution to journalArticleAcademicpeer-review

18 Downloads (Pure)

Abstract

Background: Approximately 50% of individuals with psychosis spectrum disorders (PSD) experience visual hallucinations and deficits in visual processing. Cerebral blood flow (CBF) alterations have been identified in the occipital lobe (OL) and fusiform gyrus (FG) in PSD. However, prior studies neither report on cytoarchitectonic subregions of the OL or FG, nor their correlations with cognition. Moreover, perfusion differences across neurobiologically defined psychosis Biotypes in these regions are not investigated yet. Methods: ExploreASL and FreeSurfer were used to extract perfusion measures from pseudo-continuous arterial spin labeling scans of visual (hOc1-hOc3v, middle temporal area (MT)) and fusiform (FG2-FG4) subregions in 122 bipolar disorder with psychosis (BP), 179 schizoaffective disorder (SAD), 203 schizophrenia (SZ), and 350 healthy controls (NC), as well as psychosis Biotypes (BT1-3). The data was adjusted for scanner effects using ComBat. Analyses were co-varied for total gray matter CBF. We used R to perform statistical comparisons across PSD and NC and across Biotypes. Partial Spearman correlation was performed between CBF and cognitive measures. Benjamini & Hochberg correction was used to correct for multiple comparisons. Results: PSD exhibited greater perfusion in MT and FG2 compared to NC. Perfusion significantly differed across psychosis Biotypes in hOc1 but not across diagnostic groups. Higher MT and FG4 perfusion in PSD were associated with worse overall cognitive performance. Conclusions: Visual and fusiform subregions demonstrate significant perfusion alterations which may indicate neurovascular deficits in PSD. Moreover, these perfusion alterations may contribute to cognitive impairments and visual abnormalities in psychosis.
Original languageEnglish
Article number1566184
JournalFrontiers in psychiatry
Volume16
DOIs
Publication statusPublished - 2025

Keywords

  • V5/MT
  • arterial spin labeling
  • cerebral blood flow
  • cognition
  • fusiform gyrus
  • psychosis spectrum disorders

Fingerprint

Dive into the research topics of 'Cerebral perfusion differences in the visual cortex and fusiform subregions across the psychosis spectrum'. Together they form a unique fingerprint.

Cite this